2-[3,5-Dichloro-4-(1-cyano-1-methylethyl)phenyl]-2,3,4,5-tetrahydro-3,5-dioxo-1,2,4-triazine-6-carboxylic acid → 2,6-dichloro-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)-alpha,alpha-dimethylbenzeneacetonitrile
反応式
[Cl:1][C:2]1[CH:3]=[C:4]([N:14]2[C:19](=[O:20])[NH:18][C:17](=[O:21])[C:16](C(O)=O)=[N:15]2)[CH:5]=[C:6]([Cl:13])[C:7]=1[C:8]([C:11]#[N:12])([CH3:10])[CH3:9]>SCC(O)=O>[Cl:13][C:6]1[CH:5]=[C:4]([N:14]2[C:19](=[O:20])[NH:18][C:17](=[O:21])[CH:16]=[N:15]2)[CH:3]=[C:2]([Cl:1])[C:7]=1[C:8]([CH3:10])([CH3:9])[C:11]#[N:12]参加物
3
反応条件
- 温度
- 100 °C
実験手順
A suspension of intermediate (6) (0.28 mole) in mercaptoacetic acid (250 ml) was stirred for 4 hours at 100° C., then allowed to cool to RT and stirred overnight. The reaction mixture was poured out onto crushed ice and this mixture was extracted with CH2Cl2. The separated organic layer was dried, filtered and the solvent evaporated. Toluene was added and azeotroped on the rotary evaporator. The residue was purified by short column chromatography over silica gel (eluent: CH2Cl2/CH3OH 98/2). The pure fractions were collected and the solvent was evaporated. The residue was stirred in DIPE, filtered off, washed with DIPE, then dried, yielding 36.8 g (41%) of 2,6-dichloro-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)-α,α-dimethylbenzeneacetonitrile. The filtrate was stirred in DIPE and the resulting precipitate was filtered off, washed with DIPE, and dried, yielding 2.5 g (3%) of 2,6-dichloro-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)-α,α-dimethylbenzeneacetonitrile (intermediate 7).